Literature DB >> 17168655

Arsenic trioxide in hematological malignancies: the new discovery of an ancient drug.

A Bonati1, V Rizzoli, P Lunghi.   

Abstract

Currently, Arsenic Trioxide (ATO) is considered the treatment of choice for patients with relapsed acute promyelocytic leukemia (APL). Recently, a durable remission with minimal toxicity by single agent ATO or ATO + ATRA in newly diagnosed APL was reported by different groups. These regimens have minimal toxicity and can be administered on an outpatient basis after remission induction, thus they could become a real, less toxic and more economic option to ATRA + anthracyclines in particular in low risk APL, or in patients that cannot undergo chemotherapy because of age or comorbid conditions and in patients that refuse chemotherapy. Significantly, these therapies are a successful attempt to cure a tumoral disease without chemotherapy. The results of clinical trials of ATO administration as single agent in multiple myeloma (MM) and myelodisplastic syndromes (MDS) were encouraging and showed clinical effects but they were not close to APL success. On the contrary, results of clinical trials to treat non-APL acute myeloid leukemia (AML) were disappointing. We suggest that a combination therapy with drugs targeting specific pro-survival molecules or capable to enhance pro-apoptotic pathways may lead to an improvement of ATO efficacy against hematological malignancies, in particular AML. Our pre-clinical studies showed that ATO is capable to induce cell death in acute leukemia cells but the apoptotic function is limited since it can induce also a mechanism of cell defense by activating pro-survival molecules such as MEK-ERK, Bcl-xL, Bcl-2. By combining ATO with specific MEK inhibitors, we demonstrated that the block of MEK-ERK phosphorylation, the induction of Bad de-phosphorylation, and activation of p53AIP1 apoptotic pathway interrupt the pro-survival mechanisms of ATO and kill the leukemic cells by apoptotic synergism. Our results provide an experimental basis for combined or sequential treatment with MEK inhibitors and ATO in AML. The renaissance of ATO as a drug in moderne medicine may be considered, together with ATRA success, a victory of empirical analysis, that had (and has) great impact on Chinese culture.

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Year:  2006        PMID: 17168655     DOI: 10.2174/138920106779116829

Source DB:  PubMed          Journal:  Curr Pharm Biotechnol        ISSN: 1389-2010            Impact factor:   2.837


  7 in total

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2.  Reactive oxygen species are not required for an arsenic trioxide-induced antioxidant response or apoptosis.

Authors:  Alejo A Morales; Delia Gutman; Pedro J Cejas; Kelvin P Lee; Lawrence H Boise
Journal:  J Biol Chem       Date:  2009-03-11       Impact factor: 5.157

3.  Synergistic anticancer effects of arsenic trioxide with bortezomib in mantle cell lymphoma.

Authors:  Hyun Joo Jung; Zheng Chen; Nami McCarty
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4.  Consolidation therapy of arsenic trioxide alternated with chemotherapy achieves remarkable efficacy in newly diagnosed acute promyelocytic leukemia.

Authors:  Cheng-Cheng Liu; Hua Wang; Wei-da Wang; Meng-Yuan Zhu; Qi-Rong Geng; Yue Lu
Journal:  Onco Targets Ther       Date:  2015-11-12       Impact factor: 4.147

5.  Arsenic Trioxide and Venetoclax Synergize against AML Progenitors by ROS Induction and Inhibition of Nrf2 Activation.

Authors:  Dinh Hoa Hoang; Ralf Buettner; Melissa Valerio; Lucy Ghoda; Bin Zhang; Ya-Huei Kuo; Steven T Rosen; John Burnett; Guido Marcucci; Vinod Pullarkat; Le Xuan Truong Nguyen
Journal:  Int J Mol Sci       Date:  2022-06-12       Impact factor: 6.208

6.  Targeting PML-RARα and Oncogenic Signaling Pathways by Chinese Herbal Mixture Tien-Hsien Liquid in Acute Promyelocytic Leukemia NB4 Cells.

Authors:  Chih-Jung Yao; Chia-Ming Yang; Shuang-En Chuang; Jiann-Long Yan; Chun-Yen Liu; Suz-Wen Chen; Kun-Huang Yan; Tung-Yuan Lai; Gi-Ming Lai
Journal:  Evid Based Complement Alternat Med       Date:  2011-02-20       Impact factor: 2.629

7.  Effects of arsenic on osteoblast differentiation in vitro and on bone mineral density and microstructure in rats.

Authors:  Cheng-Tien Wu; Tung-Ying Lu; Ding-Cheng Chan; Keh-Sung Tsai; Rong-Sen Yang; Shing-Hwa Liu
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  7 in total

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